Canonical Allele Identifier: CA2689596913

Gene: CDKN2A

Linked Data

• gnomAD v4: 9-21968092-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968097dup , CM000671.2:g.21968097dup	GRCh38
NC_000009.11:g.21968096dup , CM000671.1:g.21968096dup	GRCh37
NC_000009.10:g.21958096dup	NCBI36
NG_007485.1:g.31399dup , LRG_11:g.31399dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.*136dup MANE Select	ENSP00000307101.5:n.*136dup
ENST00000404796.3:c.348-61336dup	ENSP00000385916.2:n.348-61336dup
ENST00000579755.2:c.*251dup MANE Plus Clinical	ENSP00000462950.1:n.*251dup
ENST00000304494.9:c.*136dup	ENSP00000307101.5:n.*136dup
ENST00000361570.4:c.*136dup	ENSP00000355153.4:n.*136dup
ENST00000404796.2:c.348-61336dup	ENSP00000385916.2:n.348-61336dup
ENST00000498124.1:c.*300dup	ENSP00000418915.1:n.*300dup
ENST00000530628.2:c.*177dup	ENSP00000432664.2:n.*177dup
ENST00000578845.2:c.*136dup	ENSP00000467390.1:n.*136dup
ENST00000579122.1:c.*116dup	ENSP00000464202.1:n.*116dup
ENST00000579755.1:c.*251dup	ENSP00000462950.1:n.*251dup
NM_000077.4:c.*136dup , LRG_11t1:c.*136dup	NP_000068.1:n.*136dup
NM_001195132.1:c.*300dup	NP_001182061.1:n.*300dup
NM_058195.3:c.*251dup , LRG_11t2:c.*251dup	NP_478102.2:n.*251dup
NM_058197.4:c.881dup	NP_478104.2:n.881dup
XM_005251343.1:c.*136dup	XP_005251400.1:n.*136dup
XM_011517679.1:c.*136dup	XP_011515981.1:n.*136dup
NM_001363763.1:c.*136dup	NP_001350692.1:n.*136dup
NM_001363763.2:c.*136dup	NP_001350692.1:n.*136dup
NM_000077.5:c.*136dup MANE Select	NP_000068.1:n.*136dup
NM_001195132.2:c.*300dup	NP_001182061.1:n.*300dup
NM_058195.4:c.*251dup MANE Plus Clinical	NP_478102.2:n.*251dup
NM_058197.5:c.*530dup	NP_478104.2:n.*530dup